Extra Strength Pain Reliever

Product NDC
0363-0669
11-digit product format
003630669
Labeler code
0363
Product ID
0363-0669_2ce99cb7-fea1-5da2-e063-6294a90afc4e
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen tablets 500 mg
Dosage form
TABLET
Route
ORAL
Labeler
WALGREENS
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-10-13
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Extra Strength Pain Reliever
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN500 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii362O9ITL9D
Rxcui198440

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0669-01Extra Strength Pain Reliever100 in 1 BOTTLETABLET1004
0363-0669-01Extra Strength Pain Reliever1 in 1 CARTONTABLET14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-0669EXTRA STRENGTH PAIN RELIEVER (ACETAMINOPHEN TABLETS 500 MG) TABLET [WALGREENS]4Current NDC, Legacy NDC, 2 package rows20250213_c25bfe92-0196-0489-e053-2995a90abea1.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNc25bfe92-0196-0489-e053-2995a90abea14
198440acetaminophen 500 MG Oral TabletSCDc25bfe92-0196-0489-e053-2995a90abea14
198440APAP 500 MG Oral TabletSYc25bfe92-0196-0489-e053-2995a90abea14

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0363-0669-01003630669011 BOTTLE in 1 CARTON (0363-0669-01) / 100 TABLET in 1 BOTTLE1 bottle2021-10-130000-00-00NoNoCurrent